Complexity of PEDF multifunctional signaling in retinal development and diseases
retinas, and define receptor-specific signaling using siRNA and pharmacological inhibition. These receptors are broadly expressed in retinoblasts and acquire cell-type-specific patterns during retinal maturation via PEDF-independent mechanisms. LR and LRP6 also colocalize at the outer limiting membrane (OLM). Functionally, PEDF activates AKT, STAT3, ERK, and p38 and suppresses β-catenin in both HUVEC and ARPE-19 cells, while mTOR activation remains receptor-independent. LR and LRP6 couple PEDF to STAT3 and β-catenin in HUVECs, whereas in ARPE-19 cells LR links PEDF to AKT/STAT3/ERK and LRP6 to AKT/β-catenin. ATGL inhibition abolishes PEDF-induced AKT/STAT3/ERK/p38 signaling in both cell types. A 17-mer PEDF mimetic (Ppx) recapitulates these effects. These findings help define a framework for PEDF pleiotropy and highlight the OLM as a therapeutic interface.
Authors
- Colin J. Barnstable (ORCID: https://orcid.org/0000-0002-7011-4068)
- Joyce Tombran‐Tink (ORCID: https://orcid.org/0000-0002-9125-9709)
- Xiaomin Zhang (ORCID: https://orcid.org/0000-0003-4898-4152)
- Mingliang Zhang
- Xiaorong Li (ORCID: https://orcid.org/0000-0003-0641-2797)
- Changjie Ren
- Zihao Yu
Institutions
- Harrisburg University of Science and Technology (US)
- Tianjin Medical University Eye Hospital (CN)
- Tianjin Medical University (CN)
- Penn State Milton S. Hershey Medical Center (US)
Publication Details
- Journal
- Communications Biology
- Published
- 2026-05-08
- DOI
- https://doi.org/10.1038/s42003-026-10175-2
- Primary Topic
- Retinal Development and Disorders
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Natural Science Foundation of China
- Natural Science Foundation of Tianjin City